FDA Recall United States TerminatedTerminated: November 13, 2018Historical recordClass III
Swire Coca Cola USA
- Product
- Caffeine-Free Barq s Root Beer 12 Pack, 12 oz cans
- Published
- October 3, 2018
- Distribution
- Nationwide
Swire Coca Cola USA Recall: Exterior packaging correctly identifies the contents as Cherry Coca-Cola Zero, the cans contained in the fridge pack are incorrectly labeled as Cherry Coca-Cola and do not include the required notification for phenylketonurics that the beverage contains phenylalanine. - F-0854-2022
United States
TerminatedClass II
- Company
- Swire Coca Cola USA
- Product
- Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS…
- Recall date
- February 19, 2022
- Terminated
- April 27, 2022
- Source
- FDA
Reason for recall
Exterior packaging correctly identifies the contents as Cherry Coca-Cola Zero, the cans contained in the fridge pack are incorrectly labeled as Cherry Coca-Cola and do not include the required notification for phenylketonurics that the beverage contains phenylalanine.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS (144 FL OZ) in a 12-pack fridge pack carton. UPC 049000047516; UPC Cherry Coca-Cola Zero Sugar can 049000047561; Cherry Coca-Cola can 04905004. There are 2 12-packs per case. | 049000047516 | 740 cases (2 12-packs/case) | Cherry Coca-Cola Zero Sugar, MAY3022TOA 15:25 -16:15 (time stamps) 12 oz. can in a 12-pack fridge pack. Cherry Coca-Cola, MAY3022TOA, 12 oz. can (Single Cans Only) *If removed from the above 12 pack at the store for individual sale. |
Distribution
- AZ
- UT
- WY
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0854-2022
- Event ID
- 89654
- Status
- Terminated
- Classification
- Class II
- Company
- Swire Coca Cola USA
- Product description
- Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS (144 FL OZ) in a 12-pack fridge pack carton. UPC 049000047516; UPC Cherry Coca-Cola Zero Sugar can 049000047561; Cherry Coca-Cola can 04905004. There are 2 12-packs per case.
- Quantity
- 740 cases (2 12-packs/case)
- Reason
- Exterior packaging correctly identifies the contents as Cherry Coca-Cola Zero, the cans contained in the fridge pack are incorrectly labeled as Cherry Coca-Cola and do not include the required notification for phenylketonurics that the beverage contains phenylalanine.
- Recall initiation date
- February 19, 2022
- Report date
- March 16, 2022
- Classification date
- Not published in this source record
- Termination date
- April 27, 2022
- Distribution pattern
- AZ, UT, WY
- UPC, lot, and code information
- UPC 049000047516; Cherry Coca-Cola Zero Sugar, MAY3022TOA 15:25 -16:15 (time stamps) 12 oz. can in a 12-pack fridge pack. Cherry Coca-Cola, MAY3022TOA, 12 oz. can (Single Cans Only) *If removed from the above 12 pack at the store for individual sale.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Swire Coca Cola USA
Other recalls from Swire Coca Cola USA
FDA Recall United States TerminatedTerminated: July 30, 2018Historical recordClass II
Swire Coca Cola USA
- Product
- Dr. Pepper Est. 1885 Diet, 20 FL Oz (1.25 PT), 591 mL
- Published
- April 25, 2018
- Distribution
- Nationwide
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Arizona | 1 |
| Utah | 1 |
| Wyoming | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
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How to interpret this historical record
This record is preserved as published by FDA, as of April 27, 2022.
Status as reported: Terminated.
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